DIGENE HC2 DNA Collection Device - Indonesia BPOM Medical Device Registration
DIGENE HC2 DNA Collection Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104716011. The device is manufactured by QIAGEN SCIENCES LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
QIAGEN SCIENCES LLC.Country of Origin
United States
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Jan 26, 2022
Expiry Date
Mar 21, 2026
Product Type
Therapeutic Obstetric and Gynecological Equipment
Obstetric-gynecologic specialized manual instrument.
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